CV
| Title | Phenotype | Inheritance |
|---|---|---|
| ANK2 | cardiac arrhythmia, ankyrin-b-related | AD |
| ANK2 | long qt syndrome 4 | AD |
| NPPA | atrial fibrillation, familial, 6 | AD |
| NPPA | atrial standstill 2 | AR |
| CASQ2 | ventricular tachycardia, catecholaminergic polymorphic, 2 | AR |
| CACNA1C | brugada syndrome 3 | |
| CACNA1C | long qt syndrome 8 | |
| CACNA1C | timothy syndrome | AD |
| CALM1 | long qt syndrome 14 | AD |
| CALM1 | ventricular tachycardia, catecholaminergic polymorphic, 4 | AD |
| CALM2 | long qt syndrome 15 | AD |
| GJA5 | atrial fibrillation, familial, 11 | AD |
| GJA5 | atrial standstill, digenic (gja5/scn5a) | AD |
| DSG2 | arrhythmogenic right ventricular dysplasia 10 | AD |
| DSC2 | arrhythmogenic right ventricular dysplasia 11 | AD, AR |
| DSC2 | arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair | AD, AR |
| DSP | arrhythmogenic right ventricular dysplasia 8 | AD |
| KCNH2 | long qt syndrome 2, acquired, susceptibility to | AD |
| KCNH2 | long qt syndrome 2 | AD |
| KCNH2 | short qt syndrome 1 | |
| JUP | arrhythmogenic right ventricular dysplasia 12 | AD |
| JUP | naxos disease | AR |
| KCNA5 | atrial fibrillation, familial, 7 | AD |
| KCNE1 | jervell and lange-nielsen syndrome 2 | AR |
| KCNE1 | long qt syndrome 5 | AD |
| RYR2 | arrhythmogenic right ventricular dysplasia 2 | AD |
| RYR2 | ventricular tachycardia, catecholaminergic polymorphic, 1 | AD |
| TGFB3 | arrhythmogenic right ventricular dysplasia 1 | AD |
| TGFB3 | loeys-dietz syndrome 5 | AD |
| CACNB2 | brugada syndrome 4 | |
| SCN5A | {sudden infant death syndrome, susceptibility to} | AR |
| SCN5A | atrial fibrillation, familial, 10 | AD |
| SCN5A | brugada syndrome 1 | AD |
| SCN5A | cardiomyopathy, dilated, 1e | AD |
| SCN5A | heart block, nonprogressive | AD |
| SCN5A | heart block, progressive, type ia | AD |
| SCN5A | long qt syndrome 3 | AD |
| SCN5A | sick sinus syndrome 1 | AR |
| SCN5A | ventricular fibrillation, familial, 1 | |
| SCN1B | atrial fibrillation, familial, 13 | AD |
| SCN1B | brugada syndrome 5 | |
| SCN1B | cardiac conduction defect, nonspecific | |
| KCNJ2 | Andersen Tawil syndrome | AD |
| KCNJ2 | atrial fibrillation, familial, 9 | AD |
| KCNJ2 | short qt syndrome 3 | |
| KCNJ5 | long qt syndrome 13 | AD |
| SNTA1 | long qt syndrome 12 | AD |
| CAV3 | long qt syndrome 9 | AD |
| SCN2B | atrial fibrillation, familial, 14 | AD |
| ABCC9 | atrial fibrillation, familial, 12 | AD |
| PRKAG2 | wolff-parkinson-white syndrome | AD |
| PKP2 | arrhythmogenic right ventricular dysplasia 9 | AD |
| TRDN | ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness | AR |
| KCNE2 | atrial fibrillation, familial, 4 | |
| KCNE2 | long qt syndrome 6 | AD |
| AKAP9 | long qt syndrome 11 | AD |
| KCNE3 | brugada syndrome 6 | |
| HCN4 | brugada syndrome 8 | |
| HCN4 | sick sinus syndrome 2 | AD |
| KCND3 | brugada syndrome 9 | AD |
| LDB3 | left ventricular noncompaction 3 | AD |
| TRPM4 | progressive familial heart block, type ib | AD |
| CTNNA3 | arrhythmogenic right ventricular dysplasia, familial, 13 | AD |
| SCN3B | atrial fibrillation, familial, 16 | AD |
| SCN3B | brugada syndrome 7 | AD |
| SCN4B | atrial fibrillation, familial, 17 | AD |
| SCN4B | long qt syndrome 10 | AD |
| KCNQ1 | {long qt syndrome 1, acquired, susceptibility to} | AD |
| KCNQ1 | atrial fibrillation, familial, 3 | AD |
| KCNQ1 | jervell and lange-nielsen syndrome | AR |
| KCNQ1 | long qt syndrome 1 | AD |
| KCNQ1 | short qt syndrome 2 | AD |
| GPD1L | brugada syndrome 2 | |
| TMEM43 | arrhythmogenic right ventricular dysplasia 5 | AD |
| CACNA2D1 | Short QT syndrome | AD |
| CALM3 | Ventricular tachycardia, catecholaminergic polymorphic 6 | AD |
| CALM3 | Long QT syndrome 16 | AD |
| KCNJ8 | Brugada syndrome | #N/A |
| KCNJ8 | ventricular fibrillation with early repolarization | #N/A |
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